Azo dyestuffs and process for their manufacture



Patented Dec. 28, 1937 UNITED STATES A? "if.

AZO DYESTUFFS AND PROCESS FOR THEIR MANUFACTURE Walter Wehrli, Basel, Switzerland, assignor to the firm of Chemical Works formerly Sandoz,

Basel, Switzerland No Drawing. Application July 22, 1935, Serial No. 32,671. In Germany July 28, 1934 15 Claims.

The present invention relates to new azo dyestuffs and to a process for their manufacture.

It has been found that new azo dyestuffs ca pable of forming complex metal compounds on after-treatment with metal yielding agents can be prepared by coupling a diazo compound prepared from an amine of the aromatic series and containing in the ortho. position to the diazotizable amino group at least one group of the general formula acylI acyl II wherein acyl I represents sulphoalkyl, sulphoaryl and sulphoaralkyl and acyl II represents an organic acyl radical, with a coupling component or an azo dyestuff capable of coupling, and by subjecting the azo dyestuff thus obtained to a treatment with saponifying agents in order to split off the acyl group II. In this manner azo dyestuffs will be obtained which possess the general formula wherein R1 represents alkyl, aryl and aralkyl, R2 represents a radical-of an aromatic amine, R3 represents a radical of an aromatic, heterocyclic or aliphatic compound and X represents a group contiguous to the azo group and selected from the class consisting of hydroxy, alkoxy, carboxy, amino, alkylamino, aralkylamino and arylamino groups.

The azo-dyestuffs prepared by the present process can like the; respective o-hydroxy-azo dyestuffs be afterchromedon the fibre, whereby the shade becomes deeper and the properties become improved. By treating the new dyestufis in substance with compounds yielding chromium, copper or other suitable metals, they bind the metal in complex form and give Water-soluble or insoluble metal-containing dyestuffs that can be used for various purposes, for example for dyeing textiles or leather or for the manufacture of lakes and varnishes.

The diazo compounds which can be used in the present process are prepared in the usual manner from amines of the general formula acyl N acyl II wherein R represents an aromatic nucleus,whi ch may contain substituents such as halogen, alkyl, sulpho, nitro, hydroxy, carboxy, alkoxy, alkylamino, acylamino, arylamino, aralkylamino groups. The diacylated amino group may contain identical or different acyl groups, whereby acyl I must be a radical of an alkylsulphonic acid, such as methane sulphonic acid, ethane sulphonic acid etc., or of an aryl sulphonic acid such as benzene sulphonic acid, toluene sulphonic acid, naphthalene sulphonic acid, etc., which may be substituted in the aryl nucleus and contain groups such as halogen, nitro, acylamino, alkylamino, hydroxy, alkoxy, carboxy etc., or of an aralkylsulphonic acid such as benzylsulphonic acid or its derivatives. The acyl group II may be one of the above cited radicals or be derived from an organic carboxylic acid such as acetic acid, formic acid, benzoic acid, naphthoic acid, oxalic acid etc. r

The diazotization of the o-aminodiacylaminoderivatives is carried out in the usual manner, and the diazo compounds obtained are coupled in an alkaline, neutral or acid medium with such compounds of the aliphatic, aromatic or heterocyclic series that contain at ,least one hydroxy, alkoxy, carboxy, amino, alkylamino, aralkylamino or arylamino group and are able to couple with the diazo compounds in an ortho-position tonne of the groups listed above.

Such compounds are for example the derivatives of the aceto acetic acid, hydroxy-, alkoxy-, aminoand amino-hydroxy compounds of the benzene, naphthalene, anthracene and carbazol series, their sulphonic and carboxylic acids and their halogenated, nitrated, alkyla'te'd and hydroxalkylated derivatives.

It is further possible to use coupling-components such as azo dyestuffs containing a hydroxy, alkoxy, carboxy, amino, alkylated, aralkylated or acylated amino group and which couple with diazo compounds in orthc-position to the above listed groups.

Instead of coupling the diazo compound prepared from an o-amino-diacylamino compound with an already prepared azo dyestufi, it is also possible to first couple the said diazo compound with such a coupling component that is able to copulate several times and to combine the intermediate monoazo dyestufi thus obtained with any diazo compound in order to produce a polyazo dyestuff. Such polyazo dyestuffs can also be transformed into their complex metal compounds by the known processes.

The elimination of the acyl rest II from the monoor polyazo dyestuffs prepared according to the processes described above, occurs very easily on treatment with saponifying agents, without influence on the acyl rest I. If the formation of the dyestuff has been carried out in a carbonate alkaline medium, it is generally suflicient to heat it for a certain time with the mother liquor in order to obtain a complete splitting of the acyl group II. By heating the diacylamino dyestuffs before or after their isolation with a diluted caustic soda lye, the saponification and elimination of the acyl rest II occurs very rapidly.

The dyestuffs prepared according to the present invention are isolated from the reaction medium in which they have been prepared by the usual methods, say by salting them out or by precipitating them from their solutions by means of acids.

As the present invention allows to prepare a great number of different dyestuffs, their coloration in dry state may vary from yellow to dark shades. They can be used for various purposes and dye textile fibres of cellulosic or animal origin yellow to black shades.

One object of the present invention is, therefore, a process for the manufacture of azo dyestufis comprising the steps of diazotizing an o-amino-diacyl-amino compound of the aromatic series of the above cited constitution, coupling it with such a coupling component of the aliphatic, aromatic or heterocyclic series containing at least one hydroxy, alkoxy, carboxy, amino, alkylamino, aralkylamino or arylamino group and being able to couple with the diazo compound in an ortho-position to the above said groups, and subjecting the diacylamino-azo dyestuff thus obtained to a treatment with saponifying agents in order to eliminate one of the acyl groups.

Still another object of the present invention are the azo dyestuffs of the general formula N R acyl X wherein R1 represents alkyl, aryl and aralkyl, R2 represents a radical of an aromatic or heterocyclic compound, R3 represents a radical of an aromatic, aliphatic or heterocyclic compound, and X represents a group contiguous to the azo group and selected from the class consisting of hydroxy, alkoxy, carboxy, amino, alkylamino, aralkylamino and arylamino groups.

Still another object of the present invention are the azo dyestufis of the general formula wherein R1 represents alkyl, aryl and aralkyl, R2 represents a radical of an aromatic compound, R3 represents a radical of an aromatic, aliphatic or heterocyclic compound, and X represents a group contiguous to the azo group and selected from the class consisting of hydroxy, alkoxy, carboxy, amino, alkylamino, aralkylamino and arylamino groups.

Still another object of the present invention is a process for dyeing textile fibres and leather fast tints, consisting in dyeing the textile fibres with monoacylaminoazo dyestufis and aftertreating the dyeings thus obtained with compounds yielding chromium or copper, preferably in presence of acids.

Example 1 43 parts of 2-di-p-toluenesulphamino-5-methyl-l-aminobenzene are diazotized in the usual manner with 6.9 parts of sodium nitrite and 25 parts of hydrochloric acid and coupled in presence of sodium carbonate with 25.6 parts of 4- sulphophenylmethylpyrazolone. After the coupling has occurred, the precipitated dyestuff, which is difiicultly soluble in water is filtered, pasted'with some water and heated up to 90 C. with a 5% aqueous solution of caustic soda. During this treatment the dyestuff goes in solution andthe elimination of a p-toluene-sulpho radical has soon occurred. The reaction mixture is then cooled down, neutralized with hydrochloric acid and the precipitated dyestuiT filtered and dried.

In the dry form it is a yellow powder, dyeing Wool from an acid bath yellow shades, which become transformed by afterchroming into a brownish-red.

By using in this example instead of 4-sulphophenylmethylpyrazolone other sulphonated or carboxylated pyrazolone derivatives, similar products will be obtained, for instance when 2, 5- dichloro-4-sulphophenylmethylpyrazolone is employed, a dyestufif will be obtained, which dyes Wool from an acid bath greenish-yellow shades.

By using as coupling component the Neville- Winther acid instead of the pyrazolone a dyestuff will be obtained, which is a red powder, dyeing wool orange-red shades, which become violet on after-chroming.

Similar tints will be obtained with dyestuffs prepared from other naphtholmonosulphonic acids such as 1, 5-naphtholsulphonic acid, 1, 3- naphtholsulphonic. acid, 2, fi naphtholsulphonic acid and 2, 5-naphtholsulphonic acid.

Example 2 43 parts of 2di-p-toluenesulphamino-5-methyl-l-aminobenzene are diazotized in the usual manner and coupled in presence of sodium carbonate with 30.4. parts of 1-naphth0l-3, G-disulphonic acid. The dyestufi thus obtained is then saponified as described in Example 1 and isolated. In dry state it is a violet powder dyeing wool from an acid bath orange shades, which become transformed into violet on after-chroming.

Example 3 31.8 parts of 2-acetyl-p-toluenesulphamino-5- methyl-l-aminobenzene of the formula I CH3 are diazotized in the usual manner and coupled in presence of sodium carbonate with 1,-4- naphtholmonosulphonic acid. After the coupling has occurred, 25 parts of caustic soda lye are added to the solution and the whole is heated during one hour at about 90 0., whereby the saponification of the acetyl group takes place. The solution is then neutralized with acid and the dyestuff isolated and dried. It is a red powder,

' dyeing wool from an acid bathorange-red shades. 'By after-chroming violet tints will be obtained.

The dyestufi prepared'according to the present example is identical with the dyestuff obtained according 'to Example 1 from 2-di-p-toluenesulphamino--rmethyl-l-aminobenzene and 1,4-

naphtholmonosulphonic acid.

Example 4 45 parts of 2-di-p-toluenesulphamino- 5- chloro-l-arninobenzene are diazotized in the usual manner and coupled with 22.4 parts of 2- naphthol-B-sulphonic acid. The saponification of the dyestuff thus prepared is carried out in the manner described in Example 1 and the dyestuff isolated and dried. It is a dark powder dyeing wool orange-brown shades which are transformed into violet by. after-chroming and into red shades on treatment with copper salts.

Example 5 Example 6 17.3 parts of sulphanilic acid are diazotized and coupled in the usual manner with 11 parts of resorcinol in presence of sodium carbonate. The monoazo-dyestuff thus obtained is then combined with a diazo compound prepared from 45 parts of 2-di-p-toluenesulphamino-5-chloro-l-aminobenzene and the disazo dyestuff thus produced is saponified as above described and isolated. It is a brown powder, dyeing wool from an acid bath orange-brown shades, which are transformed into brown by after-chroming.

This diazo dyestuil can easily be transformed into its chromium complex compound by treating it with chromium yielding substances. The metalliferous dyestuif thus obtained dyes wool brown shades.

Example 7 49.6 parts of 2-di-p-toluenesu1phamino-1- amino-benzene-5-sulphonic acid are diazotized in the usual manner and coupled with 14.4 parts of p-naphthol in presence of sodium carbonate. The saponification of the dyestufl thus obtained is then carried out as above described and the dyestuff isolated. It is a red powder, dyeing wool brown-red shades. By'after-chroming the same become transformed into violet shades.

Example 8 49.6 parts of Z-di-p-toluenesulphamino-1- amino-benzene-B-sulphonic acid are diazotized in the usual manner and coupled in presence of sodium carbonate with 10.8 parts of m-phenylenediamine. The saponification and isolation of the dyestuff is then carried out as above described, whereby a red-brown powder, dyeing wool orange shades, .is obtained. By afterchroming brown shades are obtained.

By coupling of the above diazo compound with phenylmethylpyrazolone and saponification of the mono-azo dyestuff, a yellow powder dyeing wool yellow shades, which become orange on after-chroming, will be obtained.

- pounds.

Example 9 37.5 parts of the compound of the formula SOzCHa o1 arediazotized and coupled in presence of soda with 22.4 parts of 1,4-naphtholsulphonic acid.

By heating the monoazo dyestuff thus obtained in soda-a1kaline mother-liquor, the saponification occurs and the dyestuff can be precipitated by acidulation of the solution. In this manner, a red powder dyeing wool orange-red shades, that become violet by after-chroming, will' be obtained.

Example 10 29.2 parts of the compound of the formula S OzOzHs l CH3 are diazotized in the usual manner and coupled in presence of sodium carbonate with 25.6 parts of 4'-sulphophenylmethylpyrazolone. The saponification and isolation of the dyestuff can be carried out in a manner described above, whereby a yellow powder, dyeing wool yellow shades, that become orange on after-chroming, will be 010- 1 tained.

Example 11 usual manner.

The same dyestufl? can be prepared by coupling the intermediate product obtained from benzidine and salicylic acid, with the non-saponified monoazo compound prepared from 2-di-p-toluenesulphamino -1- aminobenzene 5 sulphonic acid and resorcin, and subjecting the trisazodyee stuff to a saponification process.

In dry state the dyestuff is a dark powder, dyeing cotton and regenerated cellulose brown shades, which become darker when aftertreated with copper salts. The complex copper compound of this dyestuff can easily be produced in substance by treating the dyestufi with copper yielding com- The complex copper compound is a water soluble dark powder, dyeing cotton, regenerated cellulose and natural silk brown shades.

methyl-l-aminobenzene are diazotized and coupled in presence of sodium carbonate with 28.3 parts of 1-(2'- methyl 3' amino sulphophenyl)-3-methy1-5-pyrazolone. After saponification and isolation a yellow powder is obtained,

by. after-chroming. The same dyestufi will be obtained if the non-saponified monoazo dyestuff is coupled with 1-hydroxynaphthalene-4-su1- phonic acid and subjected to saponification.

5 dyeing wool yellow shades which become orange If one uses instead of l-hydroxynaphthalenewhen after-chromed. 4-su1phonic acid, the equivalent quantity of 2- The monoazo dyestuff thus obtained can fur- 5'-dichloro-4-sulpho-1-pheny1-5-pyrazolone, a ther be diazotized and coupled with any coupling disazo dyestufi will be obtained, which is an component to give disazo dyestuffs. The coupling orange-brown powder dyeing wool yellow shades, product with 1hydrOXynaphtha1ene-4-sulphonic which become brown-orange by after-chroming. acid is an orange brown powder, dyeing wool The following table illustrates further examples orange-red shades, which become brownish-red of dyestuffs with their respective shades:

Monoazo dyestufis Alter sapomficatlon shade on wool Diazo component Coupling component Dry powder Direct After-chromed O N SO2C1H02 l-naphthol-l-sulphonic acid Violet Orange-red Violet. IIqHZ 4-sulpho-phenylmethyl-pyrazolone Yellow Yellow Brownish-red.

2, 5-dichloro-4-sulphophenyl-1nethyldo do Brownish-orange.

pyrazolone. 1, 4-naphthol-sulphonic acid Orange-red Violet 1-naphthol-3, G-disulphonic acid Orange Violet. 1-(2-methyl-3-amino-5-sulphophen- Yellow Orange.

yl)-3-methy1-5-pyrazolone. 2-amino-S-naphthol-fi-sulphonic acid. Dark-brown Bluish-red Dark-blue.

NH2 1, 4-naphthol-sulphonic acid Red Orange-red Violet.

| CH3 4:) NHZ Z-naphthol-G-sulphonic acid Dark Orange-brown..- Violet.

2-naphthol-6, S-disulphonic acid Orange Red-violet.

1-hydroxy-S-phenylamino-napthalene- Dark l. Violet Dark-green.

5-sulphonic acid. l-napl1tliol-4-sulphonic acid Orange-red Bluish-violeti 4-su1ph0phenyl-methylpyrazolone. Yellow Brownish-red.

OzC1H1)2 fl-naplithol Red Brown-red Violet.

ni-phenylene-diamine Orange Brown. Phenylmethyl-pyrazolo nan Orange. Resorcinol Brown-red. p-cresol t. Corinth. N-acetyl-p-aminophenol. Brownish-ye1low Violet-brown. l-acetylarnino-hnaphthol. Brownish-rednu- Black-blue. 65 Acetoacetic anilide ellow Yellow.

70 NH: l-naphthol-4-Sulphonic acid Red Orange-red Violet.

Diazo component Coupling component After saponification shade on wool Dry powder Direct After-chromed Orangebrown. Yellow Brown-orange.

sul phop henyl-3-methylpy yl) -3-methylrazolone. fi-pyrazolonel Diazo component Coupling component i bll'Hr 2 N(SO2C H1) resorcinol :dianisidine Dork powder, on cotton violet-brown, aftertreated with copper-salts reddish brown.

SOaH- IIIHz N(SO2C7H resorcinolebenzidine-esalicyli0 acid Dark powder, orange-brown on cotton, browner with copper-salts. SOaH- Do 2-amino-5-hydroxy benzidine salicylicacid. Dark-brown powder, reddish-brown on cotton,

naphthalene-7-sulbrowner with copper-salts. phonic acid. Do resorcinol am1doazo-to111ene-m0nosu1phon1c Dark powder, on leather; reddish-brown, the

acid. complex copper-compound on leather brown. Do resorcinol -1-ammo-8-hydroxy-paphthalene- Black powder, on leather: brown, copper- 3 G-disulphonic acid. complex: violet-brown.

What I claim is:- wherein Y represents a substituent selected from 1. A process for the manufacture of azo dyethe class consisting of hydrogen, halogen, alkyl,

stuffs capable of forming complex metal compounds, comprising coupling a diazo compound prepared from an amine of the aromatic series and containing in the ortho position to the diazotizable'amino group at least one group of the general formula wherein Z represents a group selected from the class consisting of sulphoalkyl, sulphoaryl and sulphoarallryl groups and acyl represents an acid radical selected from the class consisting of aliphatic and aromatic carboxylic and sulphonic acid radicals, with a coupling component selected iromthe class consisting of pyrazolones and aromatic compounds of the benzene and naphthalene series containing at least one group selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, aralkylamino and arylamino groups and capable of coupling with the diazo compounds in an ortho position to one of these groups, and subjecting the azo dyestuffs thus obtained to a treatment with an alkali in presence of Water in order to eliminate the acyl group.

2. A process for the manufacture of azo dyestufis capable of forming complex metal com pounds, comprising coupling a diazo compound prepared from an amine of the general formula acyl allroxy, nitro, sulpho, and amino groups, Z represents a group selected from the class consisting of sulphoalkyl, sulphoaryl and sulphoaralkyl groups and acyl represents an acid radical selected from the class consisting of aliphatic and aromatic carboxylic and 'sulphonic acid radicals, with a coupling component selected from the class consisting of pyrazolones and aromatic compounds of the benzene and naphthalene series containing at least one group selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, aralkylamino and arylamino groups and capable of coupling with the diazo compounds in an ortho position to one of these groups, and subjecting the azo dyestufi thus obtained to a treatment with an alkali in presence of water in order to eliminate the acyl group.

3. A process for the manufacture of azo dyestuifs capable of forming complex metal compounds, comprising coupling a diazo compound prepared from an amineof the general formula S O -aryl N NEE YLXY one group selected from the class consisting of hydroxy, alkoxy, amino; alkylamino', aralkylamino and arylamino groups and capable of coupling with the diazo compounds in an ortho position to one of these groups, and subjecting the azo dyestuff thus obtained to a treatment with an alkali in presence of water in order to eliminate the acyl group.

4. A process for the manufacture of azo dyestuffs capable of forming complex metal compounds, comprising coupling a diazo compound prepared from an amine of the general formula S 05 benzene ecyl wherein Y represents a substituent selected from the class consisting of hydrogen, halogen, alkyl,

alkoxy, nitro, sulpho, and amino groups and acyl represents an acid radical selected from the class consisting of aliphatic and aromatic carboxylic and sulphonic acid radicals, with a coupling component selected from the class consisting of pyrazolones and aromatic compounds of the benzene and naphthalene series containing at least one group selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, aralkylaminc and arylamino groups and capable of coupling with the diazo compounds in an ortho position to one of these groups, and subjecting the azo dyestuff thus obtained to a treatment with an alkali in presence of water in order to eliminate the acyl group.

5. A process for the manufacture of azo dyestuffs capable of forming complex metal compounds, comprising coupling a diazo compound prepared from an amine of the general formula NHz wherein Y represents a substituent selected from the class consisting of hydrogen, halogen, alkyl, alkoxy, nitro, sulpho, and amino groups and acyl represents an acid radical selected from the class consisting of aliphatic and aromatic carboxylic and sulphonic acid radicals, with a. coupling component selected from the class consisting of pyrazolones and aromatic compounds of the benzene and naphthalene series containing at least one group selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, aralkylamino and arylamino groups and capable of coupling with the diazo compounds in an ortho position to one of these groups, and subjecting the azo dyestuff thus obtained to a treatment with an alkali in presence of water in order to eliminate the acyl group.

6. A process for the manufacture of azo dyestuffs capable of forming complex metal compounds, comprising coupling a diazo compound prepared from an amine of the general formula 1II=(SO2C1H1)2 v NHz I wherein Y represents a substituent selected from' the class consisting of hydrogen, halogen, alkyl, alkoxy, nitro, sulpho, and amino groups, with a coupling component selected from the class consisting of pyrazolones and aromatic compounds of the benzene and naphthalene series containing at least one group selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, aralkylamino and arylamino groups and capable of coupling with the diazo compounds in an ortho position to one of these groups, and subjecting the azo dyestufi thus obtained to a treatment with an alkali in presence of water in order to eliminate one sulphotolyl group.

'7. A process for the manufacture of an azo dyestuff, comprising diazotizing the o-aminodiacylamino-compound of the formula Iii 201111);

coupling same with 1-acetyplamino-7-hydroxynaphthalene and treating the dyestufi thus obtained with an aqueous alkali solution in order to to eliminate one sulphotolyl group.

8. A process for the manufacture of an azo dyestuff, comprising diazotizing the o-aminodiacylamino compound of the formula coupling same with I-hYdIOXYl'lEiPhthElEllG-4- sulphonic acid and. treating the dyestuff thus obtained with an aqueous alkali solution in order to eliminate one sulphotolyl group.

9. Azo dyestuffs containing in their molecule at least one sulpho group and at least one group of the general formula NH-SOz-Ri X NZN/ wherein R1 represents a group selected from the class consisting of alkyl, aryl and aralkyl groups, R2 represents a radical of an aromatic compound, R3 represents a radical selected from the class consisting of radicals of pyrazolones and aromatic compounds of the benzene and naphthalene series, and X represents a substituent contiguous to the azo group and selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, arylamino and aralkylamino groups, which dyestuffs are in dry state yellow to dark powders, dyeing textile fibres yellow to black shades and which are capable of yielding complex metal compounds useful for dyeing purposes.

10. Azo dyestuffs containing in their molecule at least one sulpho group and at least one group of the general formula q Nnsorm VX\ Rs a Y Y wherein Y represents a substituent selected from the class consisting of hydrogen, alkyl, alkoxy, halogen, nitro, sulpho, amino, alkylamino, arylamino and aralkylamino groups, R1 represents a group selected from the class consisting of alkyl, aryl and aralkyl groups, R3 represents a radical selected from the class consisting of radicals of pyrazolones, and aromatic compounds of thev benzene and naphthalene series, X represents a substituent contiguous to the azo group and selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, arylamino and aralkylamino groups, which dyestufis are in dry state yellow to dark powders, dyeing textile fibres yellow to black shades and which are capable of yielding complex metal compounds useful for dyeing purposes.

11. A20 dyestuffs containing in their molecule at least one sulpho group and at least one group of the general formula wherein Y represents a substituent selected from the class consisting of hydrogen, alkyl, alkoxy, halogen, nitro, sulpho, amino, alkylamino, arylamino and aralkylamino groups, R3 represents a radical selected from the class consisting of radicals of pyrazolones and aromatic compounds of the benzene and naphthalene series, and X represents a substituent contiguous to the azo group and selected from the class consisting of hydroxy, alkoxy, amino, alkylamino, arylamino and aralkylamino groups, which dyestuffs are in dry state yellow to dark powders, dyeing textile fibres yellow to black shades and which are capable of yielding complex metal compounds useful for dyeing purposes.

12 The azo dyestuff of the formula OOCH:

/NHS 02 07111 BIL which is in dry state a brownish-violet powder, dyeing wool brownish-violet shades which become black-blue when afterchromed.

13. The azo dyestuff of the formula 80311 which is in dry state a red powder, dyeing wool orange-red shades which become violet when afterchromed.

14. The azo dyestuff of the formula 2 5 NHSO2C7H7 H0 8- c 1 N N 30 coupling same with 2-hydroxynaphthalene-6:8- disulphonic acid and treating the dyestuff thus 45 obtained with an aqueous alkali solution in order to eliminate one sulphotolyl group.

WALTER WEI-IRLI. 

